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Polyvalent 2D Entry Inhibitors for Pseudorabies and African Swine Fever Virus.
Ziem, Benjamin; Rahn, Jessica; Donskyi, Ievgen; Silberreis, Kim; Cuellar, Luis; Dernedde, Jens; Keil, Günther; Mettenleiter, Thomas C; Haag, Rainer.
Affiliation
  • Ziem B; Institute of Chemistry and Biochemistry, Freie Universität, 14195, Berlin, Germany.
  • Rahn J; Institute of Molecular Virology and Cell Biology, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, 17493, Greifswald-Insel Riems, Germany.
  • Donskyi I; Institute of Chemistry and Biochemistry, Freie Universität, 14195, Berlin, Germany.
  • Silberreis K; Institute of Laboratory Medicine, Charité-Universitätsmedizin Berlin, 13353, Berlin, Germany.
  • Cuellar L; Institute of Chemistry and Biochemistry, Freie Universität, 14195, Berlin, Germany.
  • Dernedde J; Institute of Laboratory Medicine, Charité-Universitätsmedizin Berlin, 13353, Berlin, Germany.
  • Keil G; Institute of Molecular Virology and Cell Biology, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, 17493, Greifswald-Insel Riems, Germany.
  • Mettenleiter TC; Institute of Molecular Virology and Cell Biology, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, 17493, Greifswald-Insel Riems, Germany.
  • Haag R; Institute of Chemistry and Biochemistry, Freie Universität, 14195, Berlin, Germany.
Macromol Biosci ; 17(6)2017 06.
Article de En | MEDLINE | ID: mdl-28296132
ABSTRACT
African swine fever virus (ASFV) is one of the most dangerous viruses for pigs and is endemic in Africa but recently also spread into the Russian Federation and the Eastern border of the EU. So far there is no vaccine or antiviral drug available to curtail the infection. Thus, control strategies based on novel inhibitors are urgently needed. Another highly relevant virus infection in pigs is Aujeszky's disease caused by the alphaherpesvirus pseudorabies virus (PrV). This article reports the synthesis and biological evaluation of novel extracellular matrix-inspired entry inhibitors based on polyglycerol sulfate-functionalized graphene sheets. The developed 2D architectures bind enveloped viruses during the adhesion process and thereby exhibit strong inhibitory effects, which are equal or better than the common standards enrofloxacin and heparin as demonstrated for ASFV and PrV. Overall, the developed polyvalent 2D entry inhibitors are nontoxic and efficient nanoarchitectures, which interact with various types of enveloped viruses. Therefore they prevent viral adhesion to the host cell and especially target viruses that rely on a heparan sulfate-dependent cell entry mechanism.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Antiviraux / Maladie d'Aujeszky / Peste porcine africaine / Pénétration virale Limites: Animals / Humans Langue: En Journal: Macromol Biosci Sujet du journal: BIOQUIMICA Année: 2017 Type de document: Article Pays d'affiliation: Allemagne

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Antiviraux / Maladie d'Aujeszky / Peste porcine africaine / Pénétration virale Limites: Animals / Humans Langue: En Journal: Macromol Biosci Sujet du journal: BIOQUIMICA Année: 2017 Type de document: Article Pays d'affiliation: Allemagne